STAQ Pharma, Inc. recalls Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, De
Recalled October 22, 2025 · FDA recall D-0024-2026 · STAQ Pharma
Hazard
Labeling: Incorrect or Missing Lot and/or Exp Date · FDA Class III
Sold at
Nationwide in the U.S.
Description
Labeling: Incorrect or Missing Lot and/or Exp Date
Product
Ketamine Hydrochloride, 50mg/5 mL (10mg/mL), Injection for IV use, 50 mL syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0156-02.
Manufacturer(s)
STAQ Pharma, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →